3-methoxybenzylamine

COc1cccc(CNc2ccnc(Nc3ccccc3)c2)c1
Reaction #696
收率 53.6%750 AstraZeneca ELN dataset
COc1cccc(CNC(=O)c2ccc(CCl)cc2)c1
Reaction #2516
title compound
收率 83.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(CNCCOc2cccc(-c3noc4ccsc34)c2)c1
Reaction #8771
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)c1
Reaction #8783
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cccc(CNC[C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)OC(C)(C)C)c1
Reaction #42284
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cccc(CNC[C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)OC(C)(C)C)c1
Reaction #51493
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cccc(CNC(=O)c2ccc(C(C)=O)cc2)c1
Reaction #60017
(4-acetylphenyl)-N-[(3-methoxyphenyl)methyl]carboxamide
收率 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cccc(CNc2ncnc3cc(N)ncc23)c1
Reaction #79087
7-amino-4-(3-methoxybenzylamino)pyrido[4,3-d]pyrimidine
收率 76.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cccc(CNC(=O)c2cnc3cc(NC(=O)c4ccccc4-c4ccc(C(F)(F)F)cc4)ccc3c2)c1
Reaction #80227
title compound
收率 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
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Reaction #91393
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cccc(CNC(=O)OC(C)(C)C)c1
Reaction #206708
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(CNC(=O)c2ccc(-c3cc(-c4nnc(C)o4)ccc3C)cc2)c1
Reaction #218860
N-(3-Methoxybenzyl)-2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1cccc(CNC(=O)c2ccc(-c3cnc4c(c3)N(Cc3cc(Cl)ccc3C(F)(F)F)CCN4)cc2)c1
Reaction #236582
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cccc(CNC(=O)c2ccc3cnccc3n2)c1
Reaction #258340
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cccc(CNC(=S)NCc2cccc(OC)c2)c1
Reaction #266351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCc1cc(-c2cncc(C(=O)NCc3cccc(OC)c3)c2)c(C)[nH]c1=O
Reaction #268833
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cccc(CNC(=O)C(C)(C)CO)c1
Reaction #269780
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cccc(CNC(=O)c2ccc(-c3cc(-c4nnc(C)o4)ccc3C)cc2)c1
Reaction #290852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cccc(CNC(=O)c2ccc(CCl)cc2)c1
Reaction #291536
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1cccc(CNC[C@@H](O)[C@H](Cc2ccc(F)c(F)c2)NC(=O)OC(C)(C)C)c1
Reaction #313395
(1S,2R)-[1-(3,4-Difluoro-benzyl)-2-hydroxy-3-(3-methoxy-benzylamino)-propyl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
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